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Annals of Clinical and Translational Neurology|July 20, 2024
Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literatureCamilla Mm Strano, Luca Bosco, Christian Laurini, et al.
Neuromuscular Disorders : NMD|January 1, 2021
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark coresMatteo Garibaldi, Fabiana Fattori, Elena Maria Pennisi, et al.
European Journal of Neurology|March 15, 2022
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in ItalyMarco Luigetti, Giovanni Antonini, Andrea Di Paolantonio, et al.
Journal of Neurology|April 15, 2025
Elevated serum concentrations of GFAP in hereditary transthyretin amyloidosis since pre-symptomatic stagesDomenico Plantone, Marco Luigetti, Carlo Manco, et al.
Journal of Neurology|May 14, 2025
Ravulizumab for generalized Myasthenia Gravis: a multicenter real-life experienceElena Rossini, Vincenzo Di Stefano, Raffaele Iorio, et al.
Journal of the Peripheral Nervous System : JPNS|August 3, 2023
Quantitative sensory testing and skin biopsy findings in late-onset ATTRv presymptomatic carriers: Relationships with predicted time of disease onset (PADO)Luca Leonardi, Rocco Costanzo, Francesca Forcina, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 16, 2026
Serum peripherin as a disease biomarker in hereditary transthyretin amyloidosis: a multicenter cohort studyDomenico Plantone, Delia Righi, Angela Romano, et al.
Genes|June 2, 2021
ATTRv in Lazio-Italy: A High-Prevalence Region in a Non-Endemic CountryMarco Luigetti, Valeria Guglielmino, Giovanni Antonini, et al.
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